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The efficacy and safety of acupoint catgut embedding therapy combined with tropisetron and dexamethasone in preventing nausea and vomiting induced by 3-day cisplatin-based chemotherapy: a randomized controlled trial

The efficacy and safety of acupoint catgut embedding therapy combined with tropisetron and dexamethasone in preventing nausea and vomiting induced by 3-day cisplatin-based chemotherapy: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015838
Enrollment
Unknown
Registered
2018-04-24
Start date
2018-04-16
Completion date
Unknown
Last updated
2018-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chemotherapy-induced nausea and vomiting

Interventions

A:acupoint catgut embedding therapy
B:sham acupoint catgut embedding therapy

Sponsors

The First Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients were diagnosed as malignant tumors by pathology or cytology; 2. Patients would receive 3-day cisplatin-based (25mg/m2VDd1-3) combination chemotherapy during hospitalization; 3. Aged 18 to 70 years; 4. Eastern Cooperative Oncology Group performance status of 0–2; 5. Life expectancy of at least 3 months.(6)Participated in the study and signed informed consent.

Exclusion criteria

Exclusion criteria: cancer or metastasis in the brain; vomiting and retching within 24 h before chemotherapy; use of drugs with antiemetic activity, including benzodiazepines, within 48 h before chemotherapy; use of steroids within 72 h before chemotherapy; use of drugs (such as azole antifungal agents and clarithromycin) with possible effects on the metabolism of the study drugs within 1 week before chemotherapy; use of drugs (rifampin, phenytoin, carbamazepine and barbiturates) with possible effects on metabolism of the study drugs within 4 weeks before chemotherapy; abdominal radiotherapy within days 6 to 10 of chemotherapy; hypersensitivity to any component of the study regimen and receipt of stem cell transplantation in parallel with chemotherapy.

Design outcomes

Primary

MeasureTime frame
complete response (CR; no vomiting/retching or rescue medication);

Countries

China

Contacts

Public ContactYang Cao

The First Affiliated Hospital of Guangzhou University of Chinese Medicine

393556828@qq.com+86 13802945884

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026